PedAM
Pediatric Disease Annotations & Medicines
| Disease | splenomegaly |
| Phenotype | C0020474|familial combined hyperlipidemia |
| Sentences | 1 |
| PubMedID- 24314356 | Recent studies suggest that this rare mutation may present more often without splenomegaly in patients with familial combined hyperlipidemia or autosomal dominant hypercholesterolemia. |
Page: 1